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Ozone plastics

Weak point in macromolecule Hydrolysis in Heat Ozone Plastics 0 in... [Pg.99]

Production of hydrogen fluoride from reaction of Cap2 with sulfuric acid is the largest user of fluorspar and accounts for approximately 60—65% of total U.S. consumption. The principal uses of hydrogen fluoride are ia the manufacture of aluminum fluoride and synthetic cryoHte for the Hall aluminum process and fluoropolymers and chlorofluorocarbons that are used as refrigerants, solvents, aerosols (qv), and ia plastics. Because of the concern that chlorofluorocarbons cause upper atmosphere ozone depletion, these compounds are being replaced by hydrochlorofluorocarbons and hydrofluorocarbons. [Pg.137]

Environmental Impact of Ambient Ozone. Ozone can be toxic to plants, animals, and fish. The lethal dose, LD q, for albino mice is 3.8 ppmv for a 4-h exposure (156) the 96-h LC q for striped bass, channel catfish, and rainbow trout is 80, 30, and 9.3 ppb, respectively. Small, natural, and anthropogenic atmospheric ozone concentrations can increase the weathering and aging of materials such as plastics, paint, textiles, and mbber. For example, mbber is degraded by reaction of ozone with carbon—carbon double bonds of the mbber polymer, requiring the addition of aromatic amines as ozone scavengers (see Antioxidants Antiozonants). An ozone decomposing polymer (noXon) has been developed that destroys ozone in air or water (157). [Pg.504]

Physical Factors. Unsatuiated elastomers must be stretched for ozone cracking to occur. Elongations of 3—5% are generally sufficient. Crack growth studies (10—18) have shown that some minimum force, called the critical stress, rather than a minimum elongation is required for cracking to occur. Critical stress values are neady the same for most unsaturated mbbers. However, polychloroprene has a higher critical stress value than other diene mbbers, consistent with its better ozone resistance. It has been found that temperature, plasticization, and ozone concentration have httie effect on critical stress values. [Pg.236]

Vulcanizates of ECH homopolymer and ECH—EO copolymer are resistant to ASTM oils, aUphatic solvents, and aromatic-containing fuels, showing low swell after exposure. The polymers do not harden after exposure to these fluids, although plasticizer may be extracted. Overall, these polymers offer a good balance of heat, ozone, and fuel resistance over a broad temperature range. [Pg.555]

Chlorofluoro- Used in refrigeration and production of Refrigeration, plastic foam production, Attacks stratospheric ozone layer green-... [Pg.2174]

Rubber products may be protected against ozone attack by the use of a highly saturated rubber molecule, the use of a wax inhibitor which will "bloom" to the surface, and the use of paper or plastic wrappings to protect the surface. Despite these efforts, rubber products still crack more on the West Coast than on the East Coast of the United States. [Pg.133]

Since the mid-1950s several materials have been found effective in combating ozone-initiated degradation, in particular certain p-phenylenediamine derivatives. The actual choice of such antiozonants depends on the type of polymer and on whether or not the polymer is to be subject to dynamic stressing in service. Since antiozonants are not known to have any use in plastics materials, even those which may have certain rubber particles for toughening, they will not be dealt with further here. Anyone interested further should consult references 3-5. [Pg.143]

Besides the disinfeetion of sewage effluent, ozone is used for sterilizing industrial containers sueh as plastic bottles, where heat treatment is inappropriate. Breweries... [Pg.454]

There has been only one major use for ozone today in the field of chemical synthesis the ozonation of oleic acid to produce azelaic acid. Oleic acid is obtained from either tallow, a by-product of meat-packing plants, or from tall oil, a byproduct of making paper from wood. Oleic acid is dissolved in about half its weight of pelargonic acid and is ozonized continuously in a reactor with approximately 2 percent ozone in oxygen it is oxidized for several hours. The pelargonic and azelaic acids are recovered by vacuum distillation. The acids are then esterified to yield a plasticizer for vinyl compounds or for the production of lubricants. Azelaic acid is also a starting material in the production of a nylon type of polymer. [Pg.490]

Other elements of weather and outdoor exposure can interact with UV radiation to accelerate degradation in degradable types of plastics. They include humidity, salt spray, wind, industrial pollutants, and atmospheric impurities such as ozone, biological agents, and temperature. The wavelengths that have the most effect on plastics range from 290 to 400 nm (2,900 to 4,000 A). [Pg.106]

Chlorinated polyethylene CPEs provide a very wide range of properties from soft/ elastomeric to hard. They have inherent oxygen and ozone resistance, have improved resistance (compared to PEs) to chemical extraction, resist plasticizers, volatility, and weathering. Products do not fog at high temperatures as do PVCs and can be made flame retardant. [Pg.427]

The low concentrations of ozone normally present in the atmosphere are sufficient to cause severe oxidation and cracking in polyolefins (2-13) and many other polymers such as polystyrene (6,11,12,14.15). poly(vinyl chloride) ( y, J 2,J 6) and rubbers (11,12,17-20). Where the ozone concentration is increased by air pollution, higher altitudes or the present of electrical machinery, the rate of degradation considerably increases.The prevention of such degradation represents a matter of considerable economic interest since it can greatly improve service life of polymers and plastics. An additional application of this research is to apprise the suitability of polymers for upper atmosphere application (Space Shutle flights) where a plentitude of ozone and atomic oxygen prevails. [Pg.187]

Less than 1 pphm (parts per hundred million) of ozone in the atmosphere can severely attack non-resistant rubbers. However, there is far less, if any, problem with plastics and tests are rarely made. If required, the methods standardised for rubbers in ISO 1431 [24] could be used, which involve exposure in a special cabinet with controlled levels of ozone. [Pg.71]

Due to its gaseous nature it may have an effect on the stratospheric ozone layer [281, 402, 404]. After injection into soil for fumigation, methyl bromide rapidly diffuses through the soil pore space to the soil surface and then into the atmosphere [159,162,163,405,406]. Since a plastic sheet typically covers the soil surface, the rate of emission into the atmosphere depends upon the thickness and density of the plastic, if other conditions are the same [159, 406]. Other routes of disappearance from soil include chemical hydrolysis, methylation to soil organic matter through free radical reactions, and microbial degradation [ 136,159,405,407]. Several reports appeared on the study of the microbial transformations of methyl bromide, summarized as follows ... [Pg.390]

Somogyi, G. Effect of ozone atmosphere on the detecting properties of plastic track recorders. Radiat. Eff. 16 233-243, 1972. [Pg.672]

In moderately high concentrations ozone is very toxic when inhaled, and in lesser concentrations, it is irritating to the nose and eyes. Ozone in the lower atmosphere contributes to air pollution and smog. It can cause damage to rubber, plastics, and paints. These low concentrations can cause headaches, burning eyes, and respiratory irritation. It is particular harmful to asthmatics and the elderly with respiratory problems. [Pg.230]

Bisphenol A, a compound highly used in the production of epoxy resins and polycarbonate plastics, forms monochloro-, dichloro, trichloro-, and tetrachloro derivatives when chlorinated [127], Its reaction with ozone produces as major transformation products, catechol, orthoquinone, muconic acid derivatives of bisphenol A, benzoquinone, and 2-(4-hydroxyphenyl)-propan-2-ol [128],... [Pg.118]


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See also in sourсe #XX -- [ Pg.45 , Pg.185 ]




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